WO1993015046A1 - Carbamate und diese enthaltende pflanzenschutzmittel - Google Patents

Carbamate und diese enthaltende pflanzenschutzmittel Download PDF

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Publication number
WO1993015046A1
WO1993015046A1 PCT/EP1993/000104 EP9300104W WO9315046A1 WO 1993015046 A1 WO1993015046 A1 WO 1993015046A1 EP 9300104 W EP9300104 W EP 9300104W WO 9315046 A1 WO9315046 A1 WO 9315046A1
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WO
WIPO (PCT)
Prior art keywords
formula
alkyl
alkynyl
alkenyl
hydrogen
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PCT/EP1993/000104
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German (de)
English (en)
French (fr)
Inventor
Bernd Mueller
Hubert Sauter
Franz Roehl
Reinhard Doetzer
Gisela Lorenz
Eberhard Ammermann
Original Assignee
Basf Aktiengesellschaft
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Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=27544634&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO1993015046(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from DE4234081A external-priority patent/DE4234081A1/de
Priority claimed from DE4234028A external-priority patent/DE4234028A1/de
Priority claimed from DE4234067A external-priority patent/DE4234067A1/de
Priority claimed from DE4234012A external-priority patent/DE4234012A1/de
Priority to BR9305817A priority Critical patent/BR9305817A/pt
Priority to EP93902227A priority patent/EP0624155B2/de
Priority to AU33514/93A priority patent/AU671974B2/en
Priority to UA94085752A priority patent/UA37202C2/uk
Priority to SK907-94A priority patent/SK283351B6/sk
Application filed by Basf Aktiengesellschaft filed Critical Basf Aktiengesellschaft
Priority to US08/256,628 priority patent/US5824705A/en
Priority to DE59308508T priority patent/DE59308508D1/de
Priority to DK93902227T priority patent/DK0624155T4/da
Priority to KR1019940702612A priority patent/KR100282840B1/ko
Priority to CA002127110A priority patent/CA2127110C/en
Priority to JP51289793A priority patent/JP3883566B2/ja
Publication of WO1993015046A1 publication Critical patent/WO1993015046A1/de
Priority to FI943523A priority patent/FI120766B/fi
Priority to NO942814A priority patent/NO302467B1/no
Priority to US09/275,767 priority patent/US6075148A/en
Priority to US09/527,118 priority patent/US6252083B1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/62—Oxygen or sulfur atoms
    • C07D213/63—One oxygen atom
    • C07D213/64—One oxygen atom attached in position 2 or 6
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/20—N-Aryl derivatives thereof
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/16—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
    • C07C233/24—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
    • C07C233/25—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/90—Carboxylic acid amides having nitrogen atoms of carboxamide groups further acylated
    • C07C233/91—Carboxylic acid amides having nitrogen atoms of carboxamide groups further acylated with carbon atoms of the carboxamide groups bound to acyclic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
    • C07C251/32—Oximes
    • C07C251/50—Oximes having oxygen atoms of oxyimino groups bound to carbon atoms of substituted hydrocarbon radicals
    • C07C251/58—Oximes having oxygen atoms of oxyimino groups bound to carbon atoms of substituted hydrocarbon radicals of hydrocarbon radicals substituted by nitrogen atoms not being part of nitro or nitroso groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C259/00—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
    • C07C259/04—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids
    • C07C259/06—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to hydrogen atoms or to acyclic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06—Esters of carbamic acids
    • C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/26—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
    • C07C271/28—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring to a carbon atom of a non-condensed six-membered aromatic ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/62—Compounds containing any of the groups, X being a hetero atom, Y being any atom, e.g. N-acylcarbamates
    • C07C271/66—Y being a hetero atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C275/28—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C275/32—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C275/64—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups singly-bound to oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C313/00—Sulfinic acids; Sulfenic acids; Halides, esters or anhydrides thereof; Amides of sulfinic or sulfenic acids, i.e. compounds having singly-bound oxygen atoms of sulfinic or sulfenic groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C313/08—Sulfenic acids; Derivatives thereof
    • C07C313/18—Sulfenamides
    • C07C313/26—Compounds containing any of the groups, X being a hetero atom, Y being any atom
    • C07C313/30—Y being a hetero atom
    • C07C313/34—Y being a hetero atom either X or Y, but not both, being nitrogen atoms, e.g. N-sulfenylureas
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
    • C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
    • C07C323/39—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton at least one of the nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom
    • C07C323/43—Y being a hetero atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
    • C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
    • C07C323/46—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having at least one of the nitrogen atoms, not being part of nitro or nitroso groups, further bound to other hetero atoms
    • C07C323/47—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having at least one of the nitrogen atoms, not being part of nitro or nitroso groups, further bound to other hetero atoms to oxygen atoms
    • C—CHEMISTRY; METALLURGY
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/18—One oxygen or sulfur atom
    • C—CHEMISTRY; METALLURGY
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32—One oxygen, sulfur or nitrogen atom
    • C07D239/34—One oxygen atom
    • C—CHEMISTRY; METALLURGY
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    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52—Two oxygen atoms
    • C—CHEMISTRY; METALLURGY
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D277/34—Oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/02—Systems containing only non-condensed rings with a three-membered ring

Definitions

  • the present invention relates to carbamates and their use as crop protection agents, in particular for controlling fungi, insects, nematodes and spider mites.
  • Aniline derivatives e.g. to use the i-propyl N-phenyl-carbamate or the corresponding 3-chlorophenyl ester (GB 574 995) or the methyl N-3,4-dichlorophenyl-carbamate (BE 612 550) as crop protection agents .
  • their fungicidal activity is unsatisfactory.
  • Z means methoxy, NH 2 , NHCH 3 , N (CH 3 ) 2 , CH 3 , C 2 H 5 , CF 3 or CC1 3 ,
  • X and Y independently of one another denote hydrogen, F, Cl, Br, CF 3 , CN, N0 2 , alkoxy, alkenyloxy, alkynyloxy, alkyl, alkenyl or alkynyl or can together form an optionally substituted aromatic or heteroaromatic, alicyclic or heterocyclic, partially or fully hydrogenated ring
  • R i denotes the optionally substituted radicals alkyl, alkenyl, cyclopropyl, cyclopropylmethyl, cyclobutyl, -CH 2 -CN, -CH 2 OCH 3 , -C0 2 CH 3 or -SR 5 , O-alkyl, O-alkenyl, O-alkynyl , O-cycloalkyl, O-cycloalkenyl or 0-C0 2 alkyl,
  • B can optionally be substituted and means alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, cycloalkynyl, aryl, hetaryl, heterocyclyl, hydrogen, optionally subst.
  • Alkylaryl possibly self.
  • Alkylhetaryl optionally subst.
  • Alkylcycloalkyl optionally subst.
  • Alkylcycloalkenyl
  • R 2 and R 3 are independently hydrogen, alkyl, alkenyl, alkynyl or cycloalkyl
  • R 4 denotes hydrogen, CN, alkyl, alkenyl, alkynyl, alkoxy or cycloalkyl
  • R 5 denotes alkyl, cyclopropyl, cyclopropylmethyl or cyclobutyl and their plant-compatible acid addition products and base addition products which have good fungicidal, acaricidal, insecticidal and nematocidal activity.
  • Acids for acid addition products are e.g. B. mineral acids, such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid, nitric acid, or carboxylic acids such as formic acid, acetic acid, oxalic acid, malonic acid, lactic acid, malic acid, succinic acid, tartaric acid, citric acid, salicylic acid, p-toluenesulfonic acid, Do. - Decylbenzenesulfonic acid, but also generally proton acidic compounds, e.g. B. saccharin.
  • B. saccharin such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid, nitric acid, or carboxylic acids such as formic acid, acetic acid, oxalic acid, malonic acid, lactic acid, malic acid, succinic acid, tartaric acid, citric acid, salicylic acid, p-toluenesulfonic acid, Do.
  • Bases for base addition products are e.g. As potassium, sodium, hydroxide, carbonate, ammonium hydroxide.
  • the new compounds of the formula I can be obtained in the preparation as mixtures of stereoisomers (E / Z isomers, diastereomers, enantiomers), which in the usual way, for. B, by crystallization or chromatography, can be separated into the individual components. Both the individual Isomers and their mixtures can be used as fungicides, acaricides, nematicides or insecticides and are covered by the invention. ⁇
  • the alkyls mentioned above can be substituted and have 1 to 6 carbon atoms.
  • alkenyls and alkynyls mentioned above can be substituted and have 2 to 6 carbon atoms.
  • cycloalkyls have 3 to 10 carbon atoms and are optionally substituted, for example with 1 to 4 identical or different substituents R6.
  • aryls have 6, 10 or 14 carbon atoms and are optionally substituted, for example with 1 to 4 identical or different substituents R 6 .
  • hetaryls have 5 to 14 ring atoms, from 1 to 4 heteroatoms from the group N, 0, S, are unsaturated and optionally substituted, for example with 1 to 4 identical or different substituents R 6 .
  • heterocyclyls have 5 to 14 ring atoms, of which 1 to 4 heteroatoms from the group N, 0, S are saturated or partially unsaturated and are optionally substituted, for example with 1 to 4 identical or different substituents R 6 .
  • cycloalkenyls have 5 to 14 carbon atoms and are optionally substituted, for example with 1 to 4 identical or different substituents R6.
  • R 6 can optionally be substituted, for example with 1 to 4 identical or different substituents
  • R 7 and R 6 means, for example, hydrogen, halogen, cyano, nitro, haloalkyl, alkyl, haloalkoxy, alkenyl, alkynyl, cycloalkyl, aryl, hetaryl, heterocyclyl, cycloalkenyl , Alkoxy, alkenyloxy, alkynyloxy, cycloalkyloxy, aryloxy, hetaryloxy, heterocyclicoxy, cycloalkenyloxy, alkoximino, alkenyloximino, alkynyloximino, cycloalkyloximino, cycloalkenyloximino, aryloxycarbonyl,
  • R 7 is any substituent and means, for example, hydrogen, halogen, cyano, nitro, haloalkyl, alkyl, haloalkoxy, alkenyl, alkynyl, cycloalkyl, aryl, hetaryl, heterocyclic, cycloalkenyl, alkoxy, alkenylox, alkynyloxy, cycloalkyloxy, aryloxy , hetaryloxy, heterocyclyloxy, cyclo alkenyloxy, alkoximino, Alkenyloximino, Alkinyloximino, Cycloalkyloximino, Cycloalkenyloximino, aryloximino, Het ⁇ aryloximino, Heterocyclyloximino, alkoxycarbonyl, alkenyl polyglycosides oxycarbonyl, alkynyloxycarbonyl, cycloalkyloxycarbonyl, aryloxycarbonyl
  • alkyls mentioned above can be substituted, preferably have 1 to 6 carbon atoms and are in particular methyl, ethyl, propyl, n-propyl, i-propyl, butyl, n-butyl, i-butyl, t-butyl, s-butyl, pentyl or hexyl.
  • alkenyls mentioned above can be substituted, preferably have 2-6 carbon atoms and in particular mean ethenyl, propenyl, propen- (1) -yl, propen- (2) -yl, propen- (1) -yl- (2) , Butenyl, butene- (1) -yl, butene- (2) -yl, butene- ⁇ 3) -yl, butene- (1) -yl- (3), butene- (2) -yl- ( 2), butene- (1) -yl- (2), 2-methyl-propenyl- (1), 2-methyl-propenyl- (2), pentenyl or hexenyl.
  • alkynyls can be substituted, preferably have 2 to 6 carbon atoms and are in particular ethynyl, propynyl, propyn (1) yl, propyn (3) yl, butynyl, butyn (1) yl, butyne - (2) -yl, butin- (3) -yl, 1-methylpropine (2) -yl, pentynyl or hexynyl.
  • halogens mean fluorine, chlorine, bromine or iodine.
  • cycloalkyl radicals are preferably cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, cyclodecyl, bornanyl, norbornanyl, dicyclohexyl, bicyclo [3,3,0] octyl, bicyclo [3,2, l] octyl, bicyclo [2.2.2] octyl or bicyclo [3.3, l] nonyl.
  • cycloalkenyl radicals mentioned above preferably mean cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cyclohepteny 1, cyclooctenyl, cyclononenyl, cyclodenyl, bornenyl, norbornenyl, bicyclo [3, 3, 0] octenyl, bicyclo [3, 2 , l] octenyl, bicyclo [2, 2, 2] octenyl or bicyclo [3, 3, 1] nonenyl.
  • haloalkyl radicals are preferably C 1 -C 4 -haloalkyl, in particular C 1 -C 4 -haloalkyl such as chloromethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 1-fluoroethyl, 2-fluoroethyl 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2-dichloro-2-fluoroethyl, - 2,2,2 -Trichlorethyl or pentafluoroethyl.
  • C 1 -C 4 -haloalkyl such as chloromethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluor
  • haloalkoxy radicals are preferably C 1 -C 4 -haloalkoxy, especially C 1 -C 4 -haloalkyloxy such as chloromethyloxy, dichloromethyloxy, trichloromethyloxy, fluoromethyloxy, difluoromethyloxy, trifluoromethyloxy, chlorofluoromethyloxy, dichlorofluoromethyloxy, chlorodifluoromethyl-1-fluoromethyl-1-chloro Fluoroethyloxy, 2,2-difluoroethyloxy, 2,2,2-trifluoroethylox, 2-chloro-2-fluoroethyloxy, 2-chloro-2,2-difluoroethyloxy, 2,2-dichloro-2-fluoroethyloxy, 2,2,2- Tri-chloroethyloxy or pentafluoroethyloxy.
  • C 1 -C 4 -haloalkyloxy such as chloromethyloxy, dichloromethyl
  • aryls are preferably phenyl, 1-naphthyl, 2-naphthyl, 1-anthracenyl, 2-anthracenyl or 9-anthracenyl.
  • hetaryls are preferably furyl, 2-furyl, 3-furyl, thienyl, 2-thienyl, 3-thienyl, pyrrolyl, 1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl, isoxazolyl, 3-isoxazolyl, 4- isoxazolyl, 5-isoxazolyl, isothiozolyl, 3-isothiozolyl, 4-isothiozolyl, 5-isothiozolyl, pyrazolyl, 1-pyrazolyl, 3-pyrazolyl, 4-pyrazolyl, 5-pyrazolyl, oxazolyl, 2-oxazolyl, 4 5-oxazolyl, thiazolyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, imidazolyl, 1-imidiazolyl, 2-imidazolyl, 4-imidazolyl, 5-imidazolyl, 1,2,3-thiadiazolyl, 1,2,
  • Adjacent substituents of the heteroaromatic can be condensed to an aromatic or heteroaromatic ring, so that hetaryl also includes condensed ring systems such as B. benzofuranyl, isobenzofuranyl, 1-benzothienyl, 2-benzothienyl, indolyl, isoindolyl, benzisoxazolyl, benzoxazolyl, benzisothiazolyl, benzothiazolyl, 2-benzthiazolyl, 4-benzothiazolyl, 5-benzothiazolyl, 6-benzothiazolyl
  • heterocyclyl radicals mentioned above preferably mean 2-tetrahydrofuranyl, oxiranyl, 3-tetrahydrofuranyl, 2-tetrahydrothienyl, 3-tetrahydrothienyl, 2-pyrrolidinyl, 3-pyrrolidinyl, 3-isoxazolidinyl, 4-isoxazolidinyl, 5 Isothiazolidinyl, 4-isothiazolidinyl, 5-isothiazoldinyl, 3-pyrazolidinyl, 4-pyrazolidinyl, 5-pyrazolididinyl, 2-oxazolidinyl, 4-0xazolidinyl, 5-oxazolidinyl,
  • the invention further relates to carbamates of the formula I.
  • Z means methoxy, NH 2 , NHCH 3 , CH 3 ,
  • X and Y independently of one another are hydrogen, F, Cl, Br, CF 3 , CN, NO 2 , alkoxy, akenyloxy, alkynyloxy, alkyl, alkenyl or alkynyl or can be condensed together to form a phenyl ring,
  • R 1 denotes hydrogen, alkyl, alkenyl, alkynyl, cyclopropyl, cyclopropylmethyl, cyclobutyl, -CH 2 -CN, -CH 2 -0-CH 3 , -C0 2 CH 3 or -SR 5 ,
  • Cycloalkyl optionally subst. Cycloalkenyl, optionally subst. Heterocyclyl, optionally subst. Hetaryl, possibly subst. Naphthyl, optionally subst. Arylalkyl, optionally subst. Hetarylalkyl, optionally subst. Cycloalkylalkyl optionally subst. Cycloalkenylalkyl or optionally subst. Anthracenyl
  • R 2 and R 3 are independently hydrogen, alkyl, alkenyl, alkynyl or cycloalkyl
  • R 4 represents CN, alkyl, alkenyl, alkynyl or cycloalkyl
  • R 5 denotes alkyl, cyclopropyl, cyclopropylmethyl or cyclobutyl and their plant-compatible acid addition products and base addition products.
  • the invention further relates to carbamates of the formula II 10
  • the invention further relates to carbamates of the formula III
  • the invention further relates to carbamates of the formula VII
  • X and Y independently of one another denote hydrogen, F, Cl, Br, CF 3 , CN, N0 2 , alkoxy, alkenyloxy, alkynyloxy, alkyl, alkenyl or alkynyl or can together form an optionally substituted aromatic or heteroaromatic, alicyclic or heterocyclic, partially or fully hydrogenated ring,
  • R 1 can optionally be substituted and means alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl or -CO 2 alkyl,
  • B can optionally be substituted and means alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, cycloalkynyl, aryl, hetaryl, heterocyclyl or hydrogen,
  • R 2 and R 3 are independently hydrogen, alkyl, alkenyl, alkynyl or cycloalkyl and R 4 is hydrogen, cyano, alkyl, alkenyl, alkynyl, cycloalkyl or alkoxy, and their plant-compatible acid addition products and base addition products,
  • the invention further relates to carbamates of the formula VIII
  • the invention further relates to carbamates of the formula IX 12
  • the invention further relates to carbamates of the formula X
  • the new compounds can be produced, for example, by the following methods:
  • the nitrobenzenes 2. obtainable according to standard processes are reduced to the anilms 2.
  • z. B. with hydrogen or hydrogen carriers such.
  • the anilines 2 are converted to the carbamates 2 under alkaline conditions using methyl chloroformate.
  • the carbamates are in turn prepared from the corresponding starting materials fL analogously to Scheme 1 (Scheme 3).
  • the compounds 7. become by reaction with P (CeHs) 3 or P (0-alkyl) 3 to the phosphorus compounds ________ and _____ or oxidative (e.g. with N-methylmorpholine-N-oxide) to the carbonyl compounds 12. implemented (Scheme 4).
  • the hydroxylamines 22 are obtained which, under alkaline conditions, with an oiling agent (for example propionyl chloride) or carbamoylating agent (for example methyl isocyanate) for the compound 22 and then with an electrophile , for example with an alkylating agent, to the active ingredients 2A. can be implemented (Scheme 11).
  • an oiling agent for example propionyl chloride
  • carbamoylating agent for example methyl isocyanate
  • hydroxylamine 25 (analogous to Bamberger et al., Ann. Chem. 3_16_ (1901), 278; EP 85 890) can be used for the compound 2_ ⁇ _.
  • acylated or aminoacylated (for example with methyl isocyanate) and then alkylated to the hydroxylamine derivative 22 or alkoxyacylated (for example with chloroformate).
  • the radical halogenation of 22, for example with N-bromosuccinimide, bromine, chlorine or S0C1 2 in the presence of a radical initiator, for example azoisobutyrodinitrile or under irradiation with UV light, then gives the halide 23. (Hai Cl, Br; Scheme 12 ).
  • the halides 23. can then be converted into the compounds 2-i with the corresponding nucleophiles (Scheme 13).
  • the halides 2-3. converted radically to the dihalide 20. and then converted with H 2 0 / MeOH in the presence of AgN0 3 into the carbonyl compound H or reacted directly with N-methylmorpholine-N-oxide to the carbonyl compound H.
  • £ are from the halides.
  • the phosphonates, phosphonium salts or phosphine oxides 22. (P is the respective phosphorus-organic residue) are available (Scheme 14).
  • the carbonyl compounds 21 can then be reacted with the corresponding hydroxylamines to give the oximes 22 or in a Wittig reaction to give the olefins 2A.
  • the olefins 2A can also be obtained in a Wittig reaction starting from the phosphonates, phosphonium salts or phosphine oxides 22 (Scheme 15).
  • ureas of the formula 21 can also be obtained by alkylating ureas of the formula 41, which in turn are derived from 12 by reacting 12 with the corresponding amines or directly from 21 by aminocarbonylation (for example with dimethylcarbamoyl chloride or methyl isocyanate) are accessible (see, for example, Houben-Weyl, Volume El6a, p. 208).
  • ureas of the formula 21 can also be obtained from the N-aryl-O-alkylhydroxylamines of the formula 42 in an analogous manner by aminocarbonylation. 22
  • the hydroxylamines are 22nd from the anilines A by formation of the imines AA, oxidation of the compounds AA with m-chloroperbenzoic acid and reaction of the oxaziridines with
  • the compounds listed in the following tables can be prepared accordingly.
  • the compounds ' 1.1 from Table 15 has the following formula, for example
  • Aromatics 5.45 (s, 2H, 0-CH 2); 2.35 (s, 3H, CH 3)

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DE59308508T DE59308508D1 (de) 1992-01-29 1993-01-18 Carbamate und diese enthaltende pflanzenschutzmittel
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KR1019940702612A KR100282840B1 (ko) 1992-01-29 1993-01-18 카르바메이트및그를함유한작물보호제
EP93902227A EP0624155B2 (de) 1992-01-29 1993-01-18 Carbamate und diese enthaltende pflanzenschutzmittel
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CA002127110A CA2127110C (en) 1992-01-29 1993-01-18 Carbamates and crop protection agents containing them
AU33514/93A AU671974B2 (en) 1992-01-29 1993-01-18 Carbamates and plant-protecting agents containing them
UA94085752A UA37202C2 (uk) 1992-01-29 1993-01-18 Карбамати, проміжні сполуки, фунгіцидна композиція, спосіб боротьби з грибами
SK907-94A SK283351B6 (sk) 1992-01-29 1993-01-18 Karbamáty a fungicídne prostriedky s ich obsahom
BR9305817A BR9305817A (pt) 1992-01-29 1993-01-18 Carbamato intermediario derivados de hidroxilamina composto fungicida e processo para combater fungos
US08/256,628 US5824705A (en) 1992-01-29 1993-01-18 Carbamates and crop protection agents containing them
FI943523A FI120766B (fi) 1992-01-29 1994-07-27 Karbamaatteja ja niitä sisältäviä kasvinsuojeluaineita
NO942814A NO302467B1 (no) 1992-01-29 1994-07-28 Karbamater, plantevernmidler som inneholder disse, anvendelse derav og mellomprodukter for fremstilling av dem
US09/275,767 US6075148A (en) 1992-01-29 1999-03-25 Carbamates and crop protection agents containing them
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